Assem E S, Turner-Warwick M
Clin Exp Immunol. 1976 Oct;26(1):67-77.
The immunoglobulin class and subclass of cytophilic antibodies have been studied using peripheral leucocytes from twenty-two patients with allergic bronchopulmonary aspergillosis, aspergilloma and cryptogenic pulmonary eosinophilia. In patients with allergic bronchopulmonary aspergillosis, significantly increased histamine liberation occurred following challenge of their leucocytes with antisera to IgE, IgG2, IgG3 and IgG4 as well as with Aspergillus fumigatus antigen. The results were considerably modified if the patient was receiving corticosteroids at the time of the test. The presence of IgG2-specific antibody to A. fumigatus in the serum of one patient, capable of sensitizing donor leucocytes, was demonstrated in passive sensitization experiments. In two patients with uncomplicated aspergillomas no evidence of cytophilic antibody to any class was found although large amounts of precipitating IgG antibody was present in the serum. Two patients with aspergilloma and systemic symptoms of weight loss and fatigue (which have been interpreted by others as 'hypersensitivity' responses) had increased amounts of cytophilic antibody similar to those with allergic bronchopulmonary aspergillosis. Six patients with cryptogenic pulmonary eosinophilia were also studied. No evidence of specific antibody to A. fumigatus was found but, as a group, significantly increased histamine liberation using antisera to IgG2 was demonstrated. Individual patients also showed evidence of other classes of cytophilic antibody, one having IgE, three IgG3 and two IgG4. The relationship between heat-stable short-term sensitizing antibody (IgG STS) inducing immediate skin responses and the pattern of cytophilic antibodies found in our patients with bronchopulmonary aspergillosis having dual (immediate and late reactions) is discussed. Clinically these tests are of diagnostic value and they may be helpful in assessing symptomatic patients with aspergillomas for corticosteroid treatment.
利用22例变应性支气管肺曲霉病、曲霉肿和隐源性肺嗜酸性粒细胞增多症患者的外周血白细胞,对亲细胞性抗体的免疫球蛋白类别和亚类进行了研究。在变应性支气管肺曲霉病患者中,用抗IgE、IgG2、IgG3和IgG4抗血清以及烟曲霉抗原攻击其白细胞后,组胺释放显著增加。如果患者在测试时正在接受皮质类固醇治疗,结果会有很大改变。在被动致敏实验中,证明了一名患者血清中存在能使供体白细胞致敏的针对烟曲霉的IgG2特异性抗体。在两名无并发症的曲霉肿患者中,虽然血清中存在大量沉淀性IgG抗体,但未发现任何类别的亲细胞性抗体。两名患有曲霉肿且有体重减轻和疲劳等全身症状(其他人将其解释为“超敏反应”)的患者,其亲细胞性抗体数量增加,与变应性支气管肺曲霉病患者相似。还对6例隐源性肺嗜酸性粒细胞增多症患者进行了研究。未发现针对烟曲霉的特异性抗体证据,但作为一个群体,使用抗IgG2抗血清时组胺释放显著增加。个别患者也显示出其他类别的亲细胞性抗体证据,1例有IgE,3例有IgG3,2例有IgG4。讨论了诱导即刻皮肤反应的热稳定短期致敏抗体(IgG STS)与我们患有双重(即刻和迟发反应)支气管肺曲霉病患者中发现的亲细胞性抗体模式之间的关系。临床上,这些检测具有诊断价值,可能有助于评估有症状的曲霉肿患者是否适合接受皮质类固醇治疗。